arXiv subjects

Shuming Zeng

Publications and source records attributed to Shuming Zeng.

12 recordsLinked to original sources

arXiv2026

Dimensionality Mismatch Enables Decoupled Heat and Charge Transport

Decoupling heat and charge transport is a key challenge in thermoelectrics. Here, we identify a route to spatially separate phonon and carrier transport in quasi-one-dimensional materials through high-throughput screening of the Materials Project database. Representative Sn$_2$S$_3$ and SbTeI exhibit a strong-intrachain--weak-interchain bonding hierarchy that favors phonon propagation along the chains while suppressing transverse lattice heat transport. In contrast, transverse valence-band states provide effective interchain electronic coupling and relatively light hole transport. This mismatch between lattice and electronic transport dimensionalities produces an inverted thermal--electrical anisotropy. Across the screened candidates, interchain lattice thermal conductivity is strongly suppressed, whereas hole transport remains weakly anisotropic or even favors the interchain direction. For SbTeI, this decoupling yields a maximum $zT$ of approximately 2.1 near 900~K. These results establish dimensionality mismatch as a general strategy for decoupling phonon and carrier transport in thermoelectric materials.

cond-mat.mtrl-sci↗

arXiv2026

Beyond Janus Atomic Ordering: High-Throughput First-Principles Search for Hidden MoSO Monolayer Structures

Despite the growing interest in two-dimensional (2D) MoSO systems, existing studies have exclusively focused on conventional Janus structures. In this work, we perform high-throughput first-principles calculations to explore novel stable 2D MoSO monolayers. Combined with random sampling strategy, graph theory and group theory, we successfully screen out three novel non-Janus 2D MoSO monolayers from 1325 candidate structures, namely Reversed 2H-MoSO, Hybrid 2H-MoSO, and Hybrid 1T'-MoSO. Compared with Janus MoSO monolayers, the non-Janus MoSO counterparts possess lower binding energies, varying from -4.38 to -4.51 eV/atom. A systematic combination of dynamic, thermodynamic, and mechanical stability analyses corroborates their excellent structural robustness. Ab initio molecular dynamics (AIMD) simulations confirm their superior thermal resistance, with the structures remaining stable at temperatures beyond 2000 K. Interestingly, unlike the semiconducting Janus MoSO, the Hybrid 1T'-MoSO monolayer exhibits distinct metallic characteristics. Furthermore, we found that strain and curvature can enable controlled phase transitions of MoSO among semiconducting, semimetallic, and metallic phases. More importantly, the Hybrid 1T'-MoSO exhibits favorable HER activity with a Gibbs free energy of -0.002 eV, rendering it a promising candidate for hydrogen evolution catalysis. This work not only expands the family of 2D MoSO materials but also provides a reliable strategy for discovering stable functional 2D materials via high-throughput computation.

cond-mat.mtrl-sci↗

arXiv2026

Coupling of phase transition, anharmonicity, and thermal transport in CaSnF$_6$

Understanding the coupling between structural phase transitions and thermal transport is essential for designing functional materials with tunable properties. Here, we investigate this interplay in CaSnF$_6$ by combining first-principles calculations with a machine-learned neuroevolution potential that enables large-scale molecular dynamics simulations across a wide temperature range. The simulations accurately capture the first-order structural phase transition and associated lattice dynamics. We show that the negative thermal expansion originates from low-energy rigid unit modes involving cooperative rotations of corner-sharing [CaF$_6$]$^{4-}$ octahedra, which induce bond-angle bending and volume contraction. At the same time, strong anharmonicity, dominated by four-phonon scattering, plays a central role in suppressing lattice thermal conductivity ($\kappa_L$). Crucially, non-equilibrium simulations reveal a pronounced non-monotonic anomaly in $\kappa_L$ near the phase transition, deviating from the conventional $\sim 1/T^{\alpha}$ behavior and providing direct transport evidence of lattice reconstruction. These results establish a unified mechanism linking lattice geometry, anharmonic vibrational dynamics, and thermal transport, and highlight the potential of machine-learned potentials for bridging atomic-scale phase transitions with macroscopic transport properties.

cond-mat.mtrl-sci↗

arXiv2026

Evolution of Phonon Transport Across Structural Phase Transitions in MgAgSb

MgAgSb, a promising thermoelectric material, undergoes reversible phase transitions that drastically alter its thermal transport behavior. Using first-principles calculations, we systematically investigate the lattice thermal conductivity ($\kappa_L$) of its three phases: $\alpha$, $\beta$, and $\gamma$, revealing a progressive increase following $\alpha < \beta < \gamma$. This trend originates from distinct scattering mechanisms. Four-phonon scattering substantially suppresses the particle-like conductivity ($\kappa_p$) in the $\beta$ and $\gamma$ phases, while electron-phonon scattering provides a minor additional reduction. In contrast, the wave-like conductivity ($\kappa_c$) from coherent phonon tunneling is highest in the complex $\alpha$ phase, contributing up to 44\% of $\kappa_L$. Notably, the temperature dependence of $\kappa_L$ differs fundamentally between phases: in $\beta$, the weak $\kappa_p$ variation arises from a decreasing Gr\"{u}neisen parameter with temperature; in $\alpha$, the strong rise in $\kappa_c$ with temperature counteracts the decay of $\kappa_p$. Our findings establish a comprehensive picture of thermal transport in MgAgSb, highlighting the phase-dependent interplay between particle-like and wave-like phonon contributions.

cond-mat.mtrl-sci↗

arXiv2026

Rotational Soft Modes and Octahedral Distortion as Design Principles for Ultralow Thermal Conductivity in Halide Materials

We establish that ultralow lattice thermal conductivity in halide perovskites and related octahedral framework materials arises from two distinct and complementary mechanisms: (i) halogen-halogen-enabled rotational soft modes that reshape the low-frequency spectrum and intensify phonon scattering, and (ii) static octahedral distortions that further enhance anharmonicity and reduce phonon lifetimes. Using first-principles calculations on CsPbBr3, we demonstrate that Br-Br interactions induce rotational soft modes that decongest the phonon spectrum and enhance three- and four-phonon scattering, strongly suppressing particle-like thermal conductivity (kappa_p). Independently, static octahedral distortions further reduce kappa_p by amplifying anharmonicity while leaving wave-like conductivity (kappa_c) intact. Based on these mechanistic insights, we introduce a geometric distortion factor rho and perform a high-throughput screening that first selects materials with halogen-coordinated octahedral building blocks-ensuring the presence of rotational soft modes-and then identifies those with pronounced distortion. This strategy uncovers TaGaI8 with an ultralow kappa_L = 0.11 W/mK at room temperature. This work establishes halogen-halogen-enabled rotational soft modes and octahedral distortions as transferable design principles for octahedra-containing halides, spanning both extended frameworks and molecular-cluster motifs, for discovering ultralow-kappa_L materials.

cond-mat.mtrl-sci↗

arXiv2025

Cooperative Suppression Strategy for Dual Thermal Transport Channels in Crystalline Materials

We propose a novel design principle for achieving ultralow thermal conductivity in crystalline materials via a "heavy-light and soft-stiff" structural motif. By combining heavy and light atomic species with soft and stiff bonding networks, both particle-like ($\kappa_p$) and wave-like ($\kappa_c$) phonon transport channels are concurrently suppressed. First-principles calculations show that this architecture induces a hierarchical phonon spectrum: soft-bonded heavy atoms generate dense low-frequency modes that enhance scattering and reduce $\kappa_p$, while stiff-bonded light atoms produce sparse high-frequency optical branches that disrupt coherence and lower $\kappa_c$. High-throughput screening identifies Tl$_4$SiS$_4$ ($\kappa_p$ = 0.10, $\kappa_c$ = 0.06 W/mK) and Tl$_4$GeS$_4$ ($\kappa_p$ = 0.09, $\kappa_c$ = 0.06 W/mK) as representative candidates with strongly suppressed transport in both channels. A minimal 1D triatomic chain model further demonstrates the generality of this mechanism, offering a new paradigm for phonon engineering beyond the conventional $\kappa_p$-$\kappa_c$ trade-off.

cond-mat.mtrl-sci↗

arXiv2025

Discovery of a Robust Non-Janus Hybrid MoSH Monolayer as a Two-Gap Superconductor via High-Throughput Computational Screening

The atomic-scale determination of hydrogen positions in MoSH monolayers remains experimentally challenging, and existing studies are confined to Janus-type configurations. Here, we combine high-throughput structural screening with first-principles calculations to predict a novel non-Janus Hybrid 1T$^{'}$-MoSH monolayer, which energetically surpasses all previously reported MoSH phases with a binding energy of -3.02 eV. This structure emerges as a hybrid of MoS$_2$ and MoH$_2$, featuring alternating S and H atoms on both sides of the Mo layer. Comprehensive stability analyses confirm its robustness in energy, mechanics, dynamics, and thermodynamics (stable up to 1600 K). Remarkably, anisotropic Migdal-Eliashberg theory predicts Hybrid 1T$^{'}$-MoSH as a two-gap superconductor with a critical temperature T$_c$ of 16.34 K, driven by strong electron-phonon coupling ($\lambda$$=$1.39). Substituting Mo with Hf, Ta, or Ti drastically suppresses T$_c$ $\sim$ (0.53-2.42 K), highlighting Mo$^{'}$s unique role in enhancing superconductivity. Our work not only expands the family of 2D transition metal chalcogenides but also proposes a promising candidate for quantum technologies, bridging theoretical design to functional material discovery.

cond-mat.mtrl-sci↗

arXiv2025

Decoupling Coherent and Particle-like Phonon Transport through Bonding Hierarchy in Soft Superionic Crystals

Within the framework of the unified theory thermal transport model, the competing contributions of coherent and incoherent terms create a trade-off relationship, posing substantial challenges to achieving a reduction in overall $\rm \kappa_L$. In this work, we theoretically demonstrate that the superionic crystals X$_6$Re$_6$S$_8$I$_8$ (X = Rb, Cs) exhibit ultralow glass-like and particle-like thermal conductivities. The weak interactions between free alkali metal ions X$^+$ (X = Rb, Cs) and I$^-$ anions induce pronounced lattice anharmonicity, which enhances phonon scattering and suppresses group velocities, thereby reducing the particle-like thermal conductivity ($\rm \kappa_p$). Concurrently, the significant bonding heterogeneity within the [Re$_6$S$_8$I$_6$]$^{4-}$ clusters promotes phonon dispersion flattening and low-frequency phonon localization. The resulting discretized phonon flat bands substantially diminish the glass-like thermal conductivity ($\rm \kappa_c$). At room temperature, the total $\rm \kappa_L$ of X$_6$Re$_6$S$_8$I$_8$ (X = Rb, Cs) falls below 0.2 Wm$^{-1}$K$^{-1}$. Furthermore, the bonding characteristics between X$^+$ and I$^{-1}$ anions induce an anomalous cation mass-independent stiffening of low-frequency phonon branches in this system, resulting in counterintuitive thermal transport behavior. This work elucidates fundamental mechanisms governing heat transfer in ultralow $\rm \kappa_L$ materials and establishes novel pathways for transcending conventional thermal conductivity limitations.

cond-mat.mtrl-sci↗

arXiv2025

Decoupled anisotropic Charge-Phonon Transport Enables Exceptional n-Type Thermoelectric Performance in CuBiSCl$_2$

First-principles calculations demonstrate an exceptional decoupling of charge and thermal transport along the \textit{a}-axis in CuBiSCl$_2$. The material achieves superior electron mobility (138 cm$^2$/V$\cdot$s at 300 K) through delocalized Bi-6\textit{p}/S-3\textit{p} networks while maintaining ultralow lattice thermal conductivity (0.40 W/mK at 300 K) via Cu-dominated anharmonic phonon scattering - both optimized along the same crystallographic direction. This simultaneous optimization originates from the anisotropic bonding hierarchy where [BiSCl$_2$]$_n$ ribbons enable efficient charge transport along \textit{a}-axis, while the soft vibrational modes associated with Cu atoms strongly scatter heat-carrying phonons. The resulting high power factor (1.71 mW/mK$^2$ at 700 K) and peak \textit{ZT} of 1.57 establish CuBiSCl$_2$ as a model system that realizes the long-sought "phonon glass-electron crystal" paradigm through crystallographically engineered transport channels.

cond-mat.mtrl-sci↗

arXiv2024

Weak Host Interactions Induced Thermal Transport Properties of Metal Halide Perovskites Deviating from the Rattling Model

The low-frequency phonon branches of metal halide perovskites typically exhibit the characteristic of hardening with the increase of the cation mass, which leads to anomalous thermal transport phenomenon. However, the underlying physical mechanism is not yet understood. Here, we theoretically compare the thermal transport properties of $A_2$SnI$_6$ ($A$=K, Rb, and Cs) perovskites. The thermal transport in perovskites is widely explained using the rattling model, where ``guest'' cations inside the metal halide framework act as ``rattlers'', but this fails to explain the following phenomenon: The low-frequency phonon branch of $A_2$SnI$_6$ perovskites is insensitive to the mass of the $A^+$ cation and strongly correlated with the interaction of the $A^+$ cation with the I$^-$ anion in the octahedral structures. The failure of the rattling model stems mainly from the weak interactions between the octahedral structures. By developing a new spring model, we successfully explain the thermal transport behavior in $A_2$SnI$_6$ perovskites. Our work gives new insights into the thermal transport mechanism in metal halide perovskites, which has a guiding significance for designing extremely low thermal conductivity materials.

cond-mat.mtrl-sci↗

arXiv2023

Unexpectedly Spontaneous Water Dissociation on Graphene Oxide Supported by Copper Substrate

Water dissociation is of fundamental importance in scientific fields and has drawn considerable interest in diverse technological applications. However, the high activation barrier of breaking the O-H bond within the water molecule has been identified as the bottleneck, even for the water adsorbed on the graphene oxide (GO). Herein, using the density functional theory calculations, we demonstrate that the water molecule can be spontaneously dissociated on GO supported by the (111) surface of the copper substrate (Copper-GO). This process involves a proton transferring from water to the interfacial oxygen group, and a hydroxide covalently bonding to GO. Compared to that on GO, the water dissociation barrier on Copper-GO is significantly decreased to be less than or comparable to thermal fluctuations. This is ascribed to the orbital-hybridizing interaction between copper substrate and GO, which enhances the reaction activity of interfacial oxygen groups along the basal plane of GO for water dissociation. Our work provides a novel strategy to access water dissociation via the substrate-enhanced reaction activity of interfacial oxygen groups on GO and indicates that the substrate can serve as an essential key to tuning the catalytic performance of various two-dimensional material devices.

cond-mat.mtrl-sci↗

arXiv2022

Remarkably Enhanced Dynamic Oxygen Migration on Graphene Oxide Supported by Copper Substrate

The dynamic covalent properties of graphene oxide (GO) are of fundamental interest to a broad range of scientific areas and technological applications. It remains a challenge to access the feasible dynamic reactions for reversibly breaking/reforming covalent bonds of oxygen functional groups on GO, although these reactions can be induced by photonic or mechanical routes, or mediated by adsorbed water. Here, using the density functional theory calculations, we demonstrate the remarkably enhanced dynamic oxygen migration along the basal plane of GO supported by copper substrate (GO@copper), with the C-O bond breaking reaction and proton transfer between the neighboring epoxy and hydroxyl groups. Compared to that on GO, the energy barrier of oxygen migration on GO@copper is sharply reduced to be less than or comparable to thermal fluctuations, and meanwhile the crystallographic match between GO and copper substrate induces new oxygen migration paths on GO@copper. This work sheds light on the understanding of metal substrate-enhanced dynamic properties of GO, and evidences the strategy to tune the activity of two-dimension-interfacial oxygen groups for various potential applications.

cond-mat.mtrl-sci↗